Canonical Allele Identifier: CA2615772283

Gene: CASP5

Linked Data

• gnomAD v4: 11-105007083-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105007087del , CM000673.2:g.105007087del	GRCh38
NC_000011.9:g.104877814del , CM000673.1:g.104877814del	GRCh37
NC_000011.8:g.104383024del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260315.8:c.432del MANE Select	ENSP00000260315.3:p.Lys144AsnfsTer29
ENST00000260315.7:c.432del	ENSP00000260315.3:p.Lys144AsnfsTer29
ENST00000393141.6:c.471del	ENSP00000376849.2:p.Lys157AsnfsTer29
ENST00000418434.5:c.8-3701del	ENSP00000398130.1:n.8-3701del
ENST00000444749.6:c.258del	ENSP00000388365.2:p.Lys86AsnfsTer29
ENST00000456094.1:c.384del	ENSP00000415241.1:p.Lys128AsnfsTer29
ENST00000456200.5:c.258del	ENSP00000408455.1:p.Lys86AsnfsTer?
ENST00000526056.5:c.471del	ENSP00000436877.1:p.Lys157AsnfsTer29
ENST00000531367.5:c.8-3701del	ENSP00000434471.1:n.8-3701del
NM_001136109.1:c.258del	NP_001129581.1:p.Lys86AsnfsTer29
NM_001136110.1:c.8-3701del	NP_001129582.1:n.8-3701del
NM_001136112.1:c.471del	NP_001129584.1:p.Lys157AsnfsTer29
NM_004347.3:c.432del	NP_004338.3:p.Lys144AsnfsTer29
NR_024239.1:n.290del
NR_036562.1:n.40-4883del
XM_011543020.1:c.181+1723del	XP_011541322.1:n.181+1723del
XM_011543021.1:c.432del	XP_011541323.1:p.Lys144AsnfsTer29
NM_001136109.2:c.258del	NP_001129581.1:p.Lys86AsnfsTer29
NM_001136110.2:c.8-3701del	NP_001129582.1:n.8-3701del
NM_001136112.2:c.471del	NP_001129584.1:p.Lys157AsnfsTer29
NM_004347.4:c.432del	NP_004338.3:p.Lys144AsnfsTer29
NR_024239.2:n.290del
NR_036562.2:n.40-4883del
XM_011543021.2:c.432del	XP_011541323.1:p.Lys144AsnfsTer29
NM_004347.5:c.432del MANE Select	NP_004338.3:p.Lys144AsnfsTer29
NM_001136109.3:c.258del	NP_001129581.1:p.Lys86AsnfsTer29
NM_001136110.3:c.8-3701del	NP_001129582.1:n.8-3701del
NM_001136112.3:c.471del	NP_001129584.1:p.Lys157AsnfsTer29
NR_024239.3:n.290del
NR_036562.3:n.40-4883del